Canonical Allele Identifier: CA138414288
Gene: SUPT3H HGNC NCBI
RUNX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.45338734C>T , CM000668.2:g.45338734C>T GRCh38
NC_000006.11:g.45306471C>T , CM000668.1:g.45306471C>T GRCh37
NC_000006.10:g.45414449C>T NCBI36
NG_008020.1:g.15418C>T
NG_008020.2:g.15418C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371459.6:c.101+26467G>A (SUPT3H) MANE Select ENSP00000360514.1:n.101+26467G>A
ENST00000647337.2:c.58+9950C>T (RUNX2) MANE Select ENSP00000495497.1:n.58+9950C>T
ENST00000371432.7:c.58+9950C>T (RUNX2) ENSP00000360486.4:n.58+9950C>T
ENST00000371436.10:c.58+9950C>T (RUNX2) ENSP00000360491.6:n.58+9950C>T
ENST00000371438.5:c.58+9950C>T (RUNX2) ENSP00000360493.1:n.58+9950C>T
ENST00000371459.5:c.101+26467G>A (SUPT3H) ENSP00000360514.1:n.101+26467G>A
ENST00000371460.5:c.-51-15767G>A (SUPT3H) ENSP00000360515.1:n.-51-15767G>A
ENST00000459689.1:n.214+26467G>A (SUPT3H)
ENST00000465038.6:c.58+9950C>T (RUNX2) ENSP00000420707.2:n.58+9950C>T
ENST00000475057.5:c.101+26467G>A (SUPT3H) ENSP00000436411.1:n.101+26467G>A
ENST00000483243.5:n.297+9950C>T (RUNX2)
ENST00000483377.5:c.58+9950C>T (RUNX2) ENSP00000461357.1:n.58+9950C>T
ENST00000576263.5:c.58+9950C>T (RUNX2) ENSP00000458178.1:n.58+9950C>T
NM_001015051.3:c.58+9950C>T (RUNX2) NP_001015051.3:n.58+9950C>T
NM_001024630.3:c.58+9950C>T (RUNX2) NP_001019801.3:n.58+9950C>T
NM_001261823.1:c.-265+26467G>A (SUPT3H) NP_001248752.1:n.-265+26467G>A
NM_003599.3:c.101+26467G>A (SUPT3H) NP_003590.1:n.101+26467G>A
NM_181356.2:c.-51-15767G>A (SUPT3H) NP_852001.1:n.-51-15767G>A
NR_103532.1:n.303+9950C>T (RUNX2)
NR_103533.1:n.268+9950C>T (RUNX2)
XM_011514949.1:c.-51-15767G>A (SUPT3H) XP_011513251.1:n.-51-15767G>A
XM_011514950.1:c.101+26467G>A (SUPT3H) XP_011513252.1:n.101+26467G>A
XM_011514951.1:c.101+26467G>A (SUPT3H) XP_011513253.1:n.101+26467G>A
XM_011514952.1:c.101+26467G>A (SUPT3H) XP_011513254.1:n.101+26467G>A
XM_011514953.1:c.101+26467G>A (SUPT3H) XP_011513255.1:n.101+26467G>A
XM_011514954.1:c.101+26467G>A (SUPT3H) XP_011513256.1:n.101+26467G>A
XM_011514960.1:c.262+9950C>T (RUNX2) XP_011513262.1:n.262+9950C>T
XM_011514961.1:c.262+9950C>T (RUNX2) XP_011513263.1:n.262+9950C>T
XM_011514962.1:c.262+9950C>T (RUNX2) XP_011513264.1:n.262+9950C>T
XM_011514963.1:c.262+9950C>T (RUNX2) XP_011513265.1:n.262+9950C>T
XM_011514964.1:c.262+9950C>T (RUNX2) XP_011513266.1:n.262+9950C>T
XM_011514965.1:c.262+9950C>T (RUNX2) XP_011513267.1:n.262+9950C>T
XM_011514967.1:c.262+9950C>T (RUNX2) XP_011513269.1:n.262+9950C>T
XM_011514968.1:c.262+9950C>T (RUNX2) XP_011513270.1:n.262+9950C>T
XR_926323.1:n.774+9950C>T (RUNX2)
NM_001350324.1:c.101+26467G>A (SUPT3H) NP_001337253.1:n.101+26467G>A
NM_001350325.1:c.101+26467G>A (SUPT3H) NP_001337254.1:n.101+26467G>A
NM_001350326.1:c.-51-15767G>A (SUPT3H) NP_001337255.1:n.-51-15767G>A
NM_001350327.1:c.-73+26467G>A (SUPT3H) NP_001337256.1:n.-73+26467G>A
NM_001350329.1:c.101+26467G>A (SUPT3H) NP_001337258.1:n.101+26467G>A
NR_146632.1:n.198+26467G>A (SUPT3H)
NR_146633.1:n.260+26467G>A (SUPT3H)
NR_146634.1:n.218+26467G>A (SUPT3H)
NR_146635.1:n.116+26467G>A (SUPT3H)
XM_011514949.3:c.-51-15767G>A (SUPT3H) XP_011513251.1:n.-51-15767G>A
XM_011514951.3:c.101+26467G>A (SUPT3H) XP_011513253.1:n.101+26467G>A
XM_011514952.2:c.101+26467G>A (SUPT3H) XP_011513254.1:n.101+26467G>A
XM_011514953.3:c.101+26467G>A (SUPT3H) XP_011513255.1:n.101+26467G>A
XM_011514954.3:c.101+26467G>A (SUPT3H) XP_011513256.1:n.101+26467G>A
XM_017011369.2:c.-51-15767G>A (SUPT3H) XP_016866858.1:n.-51-15767G>A
XM_017011371.1:c.101+26467G>A (SUPT3H) XP_016866860.1:n.101+26467G>A
XM_024446572.1:c.101+26467G>A (SUPT3H) XP_024302340.1:n.101+26467G>A
XR_001743691.1:n.385+26467G>A (SUPT3H)
XR_001743692.1:n.385+26467G>A (SUPT3H)
XR_002956310.1:n.385+26467G>A (SUPT3H)
NM_001024630.4:c.58+9950C>T (RUNX2) MANE Select NP_001019801.3:n.58+9950C>T
NM_003599.4:c.101+26467G>A (SUPT3H) MANE Select NP_003590.1:n.101+26467G>A
NM_001261823.2:c.-265+26467G>A (SUPT3H) NP_001248752.1:n.-265+26467G>A
NM_001350324.2:c.101+26467G>A (SUPT3H) NP_001337253.1:n.101+26467G>A
NM_001350325.2:c.101+26467G>A (SUPT3H) NP_001337254.1:n.101+26467G>A
NM_001350326.2:c.-51-15767G>A (SUPT3H) NP_001337255.1:n.-51-15767G>A
NM_001350327.2:c.-73+26467G>A (SUPT3H) NP_001337256.1:n.-73+26467G>A
NM_001350329.2:c.101+26467G>A (SUPT3H) NP_001337258.1:n.101+26467G>A
NM_181356.3:c.-51-15767G>A (SUPT3H) NP_852001.1:n.-51-15767G>A
NR_103532.2:n.290+9950C>T (RUNX2)
NR_103533.2:n.255+9950C>T (RUNX2)
NM_001015051.4:c.58+9950C>T (RUNX2) NP_001015051.3:n.58+9950C>T
NR_146632.2:n.268+26467G>A (SUPT3H)
NR_146634.2:n.260+26467G>A (SUPT3H)
NR_146635.2:n.260+26467G>A (SUPT3H)
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